Quality Assurance Associate (Pompano Beach, FL) Position Available In Broward, Florida
Tallo's Job Summary: The Quality Assurance Associate position in Pompano Beach, FL is ideal for individuals seeking an entry-level role in biotech. Responsibilities include reviewing records, assisting in investigations, and ensuring compliance with regulations. Qualifications include a degree in Biomedical or Life Sciences, strong attention to detail, and effective communication skills. This position offers opportunities for growth in quality and regulatory compliance.
Job Description
Quality Assurance Associate (Pompano Beach, FL)
Client is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical manufacturing and drug development activities in a GMP-regulated environment. This is a great opportunity for individuals looking to begin their careers in biotech, particularly in quality and regulatory compliance.
Key Responsibilities:
Receive and qualify incoming materials and reagents according to GMP requirements
Review batch records, laboratory notebooks, and QC testing results for completeness and compliance
Assist in deviation investigations and document change control processes
Support the organization and maintenance of the electronic document control system
Ensure compliance with internal SOPs and applicable cGMP regulations
Participate in internal audits and prepare documentation for regulatory inspections
Assist with data verification and archiving of quality-related records
Contribute to creation and revisions of SOPs, forms, and controlled documents
Qualifications:
Associate’s or Bachelor’s degree in Biomedical Sciences, Life Sciences, or a related field
Candidates with degrees in Data Management, Health Information Technology, Technical Writing, Supply Chain Management, or Communications who are looking to enter the biotech industry are also encouraged to apply
Strong attention to detail and organizational skills
Effective written and verbal communication skills
Ability to review and interpret technical documents and records
Self-motivated with the ability to work independently and as part of a team
Comfortable using digital tools and electronic documentation systems
Willingness to work in a GMP-regulated laboratory environment
